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1-CHLORO-6,6-DIMETHYL-2-HEPTENE-4-YNE

Base Information Edit
  • Chemical Name:1-CHLORO-6,6-DIMETHYL-2-HEPTENE-4-YNE
  • CAS No.:635708-74-6
  • Molecular Formula:C9H13Cl
  • Molecular Weight:156.655
  • Hs Code.:
  • Mol file:635708-74-6.mol
1-CHLORO-6,6-DIMETHYL-2-HEPTENE-4-YNE

Synonyms:1-chloro-6,6-dimethyl-2-heptene-4-yne;2-Hepten-4-yne,1-chloro-6,6-dimethyl;

Suppliers and Price of 1-CHLORO-6,6-DIMETHYL-2-HEPTENE-4-YNE
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • (2Z)-1-Chloro-6,6-dimethyl-2-hepten-4-yne
  • 10mg
  • $ 180.00
  • American Custom Chemicals Corporation
  • 1-CHLORO-6,6-DIMETHYL-2-HEPTENE-4-YNE 95.00%
  • 5MG
  • $ 501.16
Total 15 raw suppliers
Chemical Property of 1-CHLORO-6,6-DIMETHYL-2-HEPTENE-4-YNE Edit
Chemical Property:
  • Boiling Point:207.5±23.0 °C(Predicted) 
  • PSA:0.00000 
  • Density:0.946±0.06 g/cm3(Predicted) 
  • LogP:2.83090 
  • Storage Temp.:Amber Vial, Refrigerator 
  • Solubility.:Chloroform (Slightly), Methanol (Slightly) 
Purity/Quality:

99% *data from raw suppliers

(2Z)-1-Chloro-6,6-dimethyl-2-hepten-4-yne *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses (2Z)-1-Chloro-6,6-dimethyl-2-hepten-4-yne is a byproduct in the synthesis of Terbinafine Hydrochloride (T107500); an orally active, antimycotic allylamine related to Naftifine. It is a specific inhibitor of squalene epoxidase, a key enzyme in fungal ergosterol biosynthesis. Also antifungal.
Technology Process of 1-CHLORO-6,6-DIMETHYL-2-HEPTENE-4-YNE

There total 1 articles about 1-CHLORO-6,6-DIMETHYL-2-HEPTENE-4-YNE which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With boron trichloride; In hexane; at 20 ℃; for 0.166667h; Further Variations:; Reagents; Temperatures; reaction time; Product distribution;
DOI:10.1016/S0040-4039(00)00511-6
Guidance literature:
With potassium carbonate; In N,N-dimethyl-formamide; at 20 - 22 ℃; for 30h;
DOI:10.1007/s11094-006-0150-3
Refernces Edit
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